Simulation of the effects of complex- formation equilibria in electrophoresis: II. Experimental verification

被引:45
作者
Svobodova, Jana [1 ]
Benes, Martin [1 ]
Hruska, Vlastimil [1 ,2 ]
Uselova, Katerina [1 ]
Gas, Bohuslav [1 ]
机构
[1] Charles Univ Prague, Fac Sci, Dept Phys & Macromol Chem, CZ-12840 Prague 2, Czech Republic
[2] Agilent Technol GmbH, Waldbronn, Germany
关键词
Complex-formation equilibria; Dynamic simulation; Enantiomer separations; Simul; 5; CE ENANTIOSEPARATION SYSTEMS; CAPILLARY-ELECTROPHORESIS; CHIRAL SEPARATION; BETA-CYCLODEXTRIN; RESOLVING AGENT; THEORETICAL ASPECTS; PEAK RESOLUTION; SINGLE-ISOMER; ENANTIOMER SEPARATIONS; BINDING CONSTANTS;
D O I
10.1002/elps.201100503
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The complete mathematical model of electromigration in systems with complexation agents introduced in the Part I of this article (V. Hruska et al., Eletrophoresis, 2012, 33, this issue), which was implemented into our simulation program Simul 5, was verified experimentally. Three different chiral selector (CS) systems differing in the type of the CS, the magnitude of the complexation constants as well as in the experimental conditions were selected for verification. The experiments and simulations were performed at various concentrations of the CSs in order to discuss the influence of the concentration of the CS on the separation. The simulated and experimental electropherograms show very good agreement in the position, shape and amplitude of the analyte peaks. The new Simul 5 Complex offers a deep insight into electrophoretical separations that take place in systems containing complexing agents, for example into enantiomer separations. Using Simul 5 Complex we were able to predict and explain the significant electromigration dispersion of analyte peaks. It was clarified that the electromigration dispersion in these systems results directly from complexation. The new Simul 5 Complex was also shown to be a useful and powerful tool for the prediction of the results of enantioseparations.
引用
收藏
页码:948 / 957
页数:10
相关论文
共 50 条
[1]   Determination of stability constants of complexes of neutral analytes with charged cyclodextrins by affinity capillary electrophoresis [J].
Benes, Martin ;
Zuskova, Iva ;
Svobodova, Jana ;
Gas, Bohuslav .
ELECTROPHORESIS, 2012, 33 (06) :1032-1039
[2]   EXPERIMENTAL-EVIDENCE FOR THE EXISTENCE OF DUOSELECTIVE (TYPE-III) ENANTIOMER SEPARATIONS IN THE CAPILLARY ELECTROPHORETIC ANALYSIS OF CHIRAL WEAK ACIDS [J].
BIGGIN, ME ;
WILLIAMS, RL ;
VIGH, G .
JOURNAL OF CHROMATOGRAPHY A, 1995, 692 (1-2) :319-325
[3]   Dynamic high-resolution computer simulation of electrophoretic enantiomer separations with neutral cyclodextrins as chiral selectors [J].
Breadmore, Michael C. ;
Kwan, Hiu Ying ;
Caslavska, Jitka ;
Thormann, Wolfgang .
ELECTROPHORESIS, 2012, 33 (06) :958-969
[4]   High-resolution computer simulations of EKC [J].
Breadmore, Michael C. ;
Quirino, Joselito P. ;
Thormann, Wolfgang .
ELECTROPHORESIS, 2009, 30 (04) :570-578
[5]  
Busby MB, 2002, ELECTROPHORESIS, V23, P456, DOI 10.1002/1522-2683(200202)23:3<456::AID-ELPS456>3.0.CO
[6]  
2-X
[7]   Comparison of five methods for the study of drug-protein binding in affinity capillary electrophoresis [J].
Busch, MHA ;
Carels, LB ;
Boelens, HFM ;
Kraak, JC ;
Poppe, H .
JOURNAL OF CHROMATOGRAPHY A, 1997, 777 (02) :311-328
[8]   Capillary electrophoretic separation of weak base enantiomers using the single-isomer heptakis-(2,3-dimethyl-6-sulfato)-β-cyclodextrin as resolving agent and methanol as background electrolyte solvent [J].
Cai, H ;
Vigh, G .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1998, 18 (4-5) :615-621
[9]   Enantioseparations by using capillary electrophoretic techniques The story of 20 and a few more years [J].
Chankvetadze, Bezhan .
JOURNAL OF CHROMATOGRAPHY A, 2007, 1168 (1-2) :45-70
[10]   ELECTROMIGRATION IN SYSTEMS WITH ADDITIVES IN BACKGROUND ELECTROLYTES .1. ADDITION OF THE NEUTRAL COMPLEXING AGENT [J].
DUBROVCAKOVA, E ;
GAS, B ;
VACIK, J ;
SMOLKOVAKEULEMANSOVA, E .
JOURNAL OF CHROMATOGRAPHY, 1992, 623 (02) :337-344